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Journal of Clinical Microbiology, August 1998, p. 2301-2307, Vol. 36, No. 8
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Evaluation of PCR, Culture, and Serology for Diagnosis of Chlamydia pneumoniae Respiratory Infections

R. P. Verkooyen,1,* D. Willemse,1 S. C. A. M. Hiep-van Casteren,2 S. A. Mousavi Joulandan,3 R. J. Snijder,2 J. M. M. van den Bosch,2 H. P. T. van Helden,4 M. F. Peeters,5 and H. A. Verbrugh1

Department of Medical Microbiology and Infectious Diseases, Erasmus University Medical Center Rotterdam, Rotterdam,1 Departments of Pulmonary Diseases2 and Medical Microbiology and Immunology,4 St. Antonius Hospital, Nieuwegein,2 Department of Medical Microbiology, Diakonessen Hospital, Utrecht,3 and Department of Medical Microbiology, St. Elisabeth Hospital, Tilburg,5 The Netherlands

Received 4 December 1997/Returned for modification 27 January 1998/Accepted 30 April 1998

We prospectively studied 156 patients with a diagnosis of community-acquired pneumonia requiring admission. Several respiratory specimens were obtained for the detection of Chlamydia pneumoniae by cell culture and PCR. Three serum samples were obtained from each patient. Serological diagnosis of a C. pneumoniae infection was determined by the microimmunofluorescence (MIF) test, the complement fixation (CF) test, and recombinant lipopolysaccharide (LPS) enzyme-linked immunosorbent assay (ELISA; referred to as the rDNA LPS ELISA). Twenty-three patients (15%) had serological results compatible with acute C. pneumoniae infection; nine (39%) of these subjects were C. pneumoniae PCR positive. Twenty-two patients (14%) had positive PCR results without serological evidence of an acute C. pneumoniae infection. An attempt was made to calculate the sensitivities and specificities of the MIF test, rDNA LPS ELISA, and PCR for the diagnosis of chlamydial community-acquired pneumonia. Several "gold standards" were defined. Generally, the sensitivities of the rDNA LPS ELISA and MIF were comparable, while the sensitivity of the CF test was shown to be very low. Independent of the gold standard used, the best PCR results were obtained with nasopharyngeal specimens. However, the predictive value of a positive C. pneumoniae PCR result for patients with community-acquired pneumonia remains unknown and may be low. Although a widely accepted gold standard is still lacking, the rDNA LPS ELISA may currently be the preferred tool for diagnosing acute respiratory Chlamydia infections in routine clinical practice. However, the MIF test remains the method of choice for determining the prevalence of C. pneumoniae infections in a given community.


* Corresponding author. Mailing address: Department of Medical Microbiology and Infectious Diseases, Erasmus University Medical Center, Rotterdam, Room Ee1720, P.O. box 1738, 3000 DR Rotterdam, The Netherlands. Phone: 31 10 463 3510. Fax: 31 10 463 4730. E-mail: Verkooyen{at}kmic.fgg.eur.nl.


Journal of Clinical Microbiology, August 1998, p. 2301-2307, Vol. 36, No. 8
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.



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